chr9:21304326:> Detail (hg38)

Information

Genome

Assembly Position
hg19 chr9:21,304,325-21,305,312 
hg38 chr9:21,304,326-21,305,313

HGVS

Type Transcript Protein
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

[No Data.]

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
<0.001 Hepatitis, Chronic NA BeFree Detail
0.002 hepatitis C NA GAD Detail
<0.001 Liver neoplasms NA BeFree Detail
0.003 Lupus Erythematosus, Systemic NA BeFree,GAD Detail
0.122 melanoma NA CTD_human,GAD Detail
0.002 Nevus NA GAD Detail
0.120 Pancreatic Neoplasm NA CTD_human Detail
<0.001 papilloma NA BeFree Detail
0.002 Respiratory Syncytial Virus Infections NA GAD Detail
0.002 Skin Neoplasms NA GAD Detail
<0.001 Hepatitis B, Chronic NA BeFree Detail
0.001 liver carcinoma NA BeFree Detail
<0.001 bronchiolitis SNPs in the innate immune genes VDR (rs10735810; P=.0017), JUN (rs11688; P=.0093... BeFree 17703412 Detail
<0.001 bronchiolitis NA BeFree Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
SNPs in the innate immune genes VDR (rs10735810; P=.0017), JUN (rs11688; P=.0093), IFNA5 (rs10757212... DisGeNET Detail
NA DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs10735810 dbSNP
Genome
hg38
Position
chr9:21,304,326-21,305,313
Variant Type
snv
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